Bronchial Asthma

Not yet recruiting

• Conditions: Other and unspecified asthma. Ayurveda Condition: TAMAKASVASAH,

• Registration Number: CTRI/2021/05/033648
• Lead Sponsor: Gurukul Campus UAU Haridwar

Brief Summary

This study is a open label, randomized, parallel group clinical trial to determine the efficacy of Kulattha Guda in Tamak Shawasa (Bronchial Asthma) for age group between 18-60 years daily for 45 days. The study will be conducted at UAU, Gurukul Campus, Haridwar on 40 patients. The assessment will be done on the basis of Subjective and Objective parameters. The study will be conducted at OPD/IPD level of P.G. Department of Kaya Chikitsa . The assessment will be done at the interval of 10 days of the clinical trial and the results obtained will be tabulated and statistically analyzed using appropriate tests.

Detailed Description

Not available

Study Timeline

• Study Start: 2021-05-22
• Last Update Posted: 2021-12-05

Recruitment & Eligibility

• Status: Not Yet Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

• Patient having classical features of Tamak Shwasa(Bronchial Asthama) will be selected.
• Age 18-60 yrs will be included irrespective of sex,religion and caste discrimination.

Exclusion Criteria

• Patients below 18 years and above 60 years.
• Bronchial Asthma associated with complications like emphysema, cor-pulmonale etc.
• Patients suffering from Pulmonary Tuberculosis, Lung cancer, Lung fibrosis, Acute & chronic Bronchitis.
• Diabetic patients.
• Severe attack of asthma.
• Cardiac disease like cardiac asthma, I.H.D. etc.
• Patient suffering from other major medical and psychiatric disorders.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
1.Shayane Shwasha piditam (Breathlessness during lying position)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
2.Aasinolabhate saukhyam (Comfort in sitting posture)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
3.Shleshman aamuchyamane Bhrusham dhukhitam (Difficult to expectorate)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
4.Shleshma Vimokshante Muhurtam sukham (Momentary relief after expectoration)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
5.Shwasakrichta (Difficulty in breathing)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
6.Ghurgurakam (Wheezing sound)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
7.Parsve Avagruhyate (Chest tightness)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
8.Ativega Kasate (Frequent bouts coughing)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.
9.Anidra (Disturbed sleep due to breathlessness)	The assessment will be done on the basis of relief in the subjective parameters with the interval of 10 days.

Secondary Outcome Measures

Name	Time	Method
1.Blood - Hb%, TLC, DLC, ESR.	2.Absolute Eosinophil Count (AEC)

Trial Locations

Locations (1)

Gurukul Campus UAU Haridwar; 🇮🇳 Hardwar, UTTARANCHAL, India

Gurukul Campus UAU Haridwar

🇮🇳Hardwar, UTTARANCHAL, India

Vandana Rawat

Principal investigator

9410772565

dr.vannurawat1993@gmail.com